Evidence map›Paper›PMID 34182560›Full record

ArticleJournal of innate immunity2021

Intestinal Epithelial Cell-Derived CD83 Contributes to Regulatory T-Cell Generation and Inhibition of Food Allergy.

Yong Yu, Qiao-Ruo Jin, Yang Mi, Jiang-Qi Liu, Zhi-Qiang Liu, Shuai Wang, Zhi-Gang Liu, Ping-Chang Yang, Peng-Yuan Zheng

Open access · goldAbstract read
In one paragraph

Article in Journal of innate immunity, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.3field-weighted citation impact, top 22% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. C5aRNPJ vaccines · 2023
    Article
  3. Article
  4. Article
  5. CD83 Regulates the Immune Responses in Inflammatory Disorders.International journal of molecular sciences · 2023
    Review
  6. Review
  7. Soluble CD83 Accelerates Wound Healing and Attenuates Inflammatory Responses Induced by Chronic Wound Fluid in a Human 3D in Vitro Wound Healing Model.Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 1 country.

Yong YuDepartment of Gastroenterology, Fifth Hospital of Zhengzhou University, Zhengzhou, China.
Qiao-Ruo JinGuangdong Provincial Key Laboratory of Regional Immunity and Diseases, Shenzhen, China.
Yang MiDepartment of Gastroenterology, Fifth Hospital of Zhengzhou University, Zhengzhou, China.
Jiang-Qi LiuLonggang ENT Hospital and Shenzhen ENT Institute, Shenzhen, China.
Zhi-Qiang LiuLonggang ENT Hospital and Shenzhen ENT Institute, Shenzhen, China.
Shuai WangLonggang ENT Hospital and Shenzhen ENT Institute, Shenzhen, China.
Zhi-Gang LiuResearch Center of Allergy and Immunology, Shenzhen University School of Medicine, Shenzhen, China.
Ping-Chang YangGuangdong Provincial Key Laboratory of Regional Immunity and Diseases, Shenzhen, China.
Peng-Yuan ZhengDepartment of Gastroenterology, Fifth Hospital of Zhengzhou University, Zhengzhou, China.
Fifth Affiliated Hospital of Zhengzhou University · CNShenzhen University · CNLonggang Central Hospital · CNKey Laboratory of Guangdong Province · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The mechanism of generation of antigen-specific regulatory T cells (Treg) is not fully understood yet. This study aimed to investigate the role of intestinal epithelial cell (IEC)-derived CD83 in the Treg generation in the intestine. In this study, the role of CD83 in the generation of Tregs was assessed in a cell-culture model and a food allergy (FA) mouse model. We found that mouse IECs expressed CD83; its levels were markedly lower in sensitized mice. Mice with CD83-deficient IECs failed to induce Tregs in the intestine. CD83 promoted the transforming growth factor-β-inducible early gene 1 (TIEG1) expression in CD4+ T cells. Toll-like receptor 4 (TLR4)/myeloid differentiation protein-2 (MD-2) complex mediated the effects of CD83 on the expression of TIEG1. Activation of the CD83/TLR4/MD-2/TIEG1 promoted the Treg generation. Concomitant administration of CD83 and specific antigens, but not either one alone, efficiently inhibited experimental FA via inducing the Treg generation in the intestine. In Conclusion, IEC expresses CD83 that is low in sensitized mice. Concomitant administration of CD83 and specific antigens efficiently inhibits FA in a murine model via inducing Tregs in the intestine. The data suggest that CD83 has translation potential in the treatment of FA.

Indexed as

Food HypersensitivityT-Lymphocytes, RegulatoryAnimalsAntigens, CDCD83 AntigenDNA-Binding ProteinsEarly Growth Response Transcription FactorsEpithelial CellsImmune ToleranceImmunoglobulinsIntestinesKruppel-Like Transcription FactorsMembrane GlycoproteinsMiceTranscription FactorsAntigens, CDCD83 AntigenDNA-Binding ProteinsEarly Growth Response Transcription FactorsImmunoglobulinsKLF10 protein, mouseKruppel-Like Transcription FactorsMembrane GlycoproteinsTranscription FactorsEpithelial cellFood allergyImmunotherapyIntestineT lymphocyte

Identifiers

PMID34182560
PMCPMC8460988
OpenAlexW3175865011

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.